Boy, Jana <br/><br/>
A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeats.  [electronic resource] 

 -  Neurobiology of disease  Feb 2010 
 - 284-93 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1095-953X 
<br/><br/><label>Standard No.: </label>10.1016/j.nbd.2009.08.002  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Age of Onset<br/>Animals<br/>Ataxin-3<br/>Brain--metabolism<br/>Chromosomal Instability--genetics<br/>Disease Models, Animal<br/>Disease Progression<br/>Gene Expression--genetics<br/>Genetic Predisposition to Disease--genetics<br/>Intranuclear Inclusion Bodies--genetics<br/>Machado-Joseph Disease--genetics<br/>Mice<br/>Mice, Transgenic<br/>Movement Disorders--genetics<br/>Mutation--genetics<br/>Nuclear Proteins--genetics<br/>Rats<br/>Sex Characteristics<br/>Transcription Factors--genetics<br/>Trinucleotide Repeats--genetics